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PRO LASER
PRO LASER - 42248-130-01 - (OCTINOXATE, TITANIUM DIOXIDE, OXYBENZONE)
Drug Information of PRO LASER
| Product NDC: | 42248-130 |
| Proprietary Name: | PRO LASER |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, OXYBENZONE |
| Active Ingredient(s): | 11.25; 9; 37.5 mL/150mL; mL/150mL; mL/150mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRO LASER
| Product NDC: | 42248-130 |
| Labeler Name: | Zenith Medicosm SL |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111201 |
Package Information of PRO LASER
| Package NDC: | 42248-130-01 |
| Package Description: | 150 mL in 1 BOTTLE (42248-130-01) |
NDC Information of PRO LASER
| NDC Code | 42248-130-01 |
| Proprietary Name | PRO LASER |
| Package Description | 150 mL in 1 BOTTLE (42248-130-01) |
| Product NDC | 42248-130 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Zenith Medicosm SL |
| Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 11.25; 9; 37.5 |
| Strength Unit | mL/150mL; mL/150mL; mL/150mL |
| Pharmaceutical Classes |
